Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Yu. G. Putsykin"'
Publikováno v:
Doklady Biological Sciences. 420:204-206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aeebab1dafe649417aee6b5349ee5b91
https://doi.org/10.1134/s0012496608030186
https://doi.org/10.1134/s0012496608030186
Publikováno v:
Pharmaceutical Chemistry Journal. 29:764-769
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77dbe294961c70b2a18efe42ab3e1d17
https://doi.org/10.1007/bf02331857
https://doi.org/10.1007/bf02331857
Publikováno v:
Russian Chemical Bulletin. 44:695-698
The synthesis and X-ray structural study of 1-(4-chlorophenyl)-3-(5-methyl-1,3-dioxan-5-yl)-(1,2), (3,4)-diepoxybutane are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd4503117a8fd850e22c52f5c56ce897
https://doi.org/10.1007/bf00698505
https://doi.org/10.1007/bf00698505
Publikováno v:
Russian Chemical Bulletin. 42:1995-2000
O-Methyloximes and nitrones of a series of substituted 4-[2-hydroxy-2-(1H-1,2,4-triazol-1-ylmethyl)cyclohexylidenemethyl]benzaldehydes have been synthesized, and their fungicidal activity has been assayed. All of them exhibit low fungicidal activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68d2d3ae9c78f151c890326b84f3706a
https://doi.org/10.1007/bf00698882
https://doi.org/10.1007/bf00698882
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a3474125a9c2b00eb653e5a451b72e8
https://doi.org/10.1002/chin.199238152
https://doi.org/10.1002/chin.199238152
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5709d3a232a2e18f65afaa4629e68f0d
https://doi.org/10.1002/chin.199446149
https://doi.org/10.1002/chin.199446149
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6df6b3e1cafefb84e88e8b4ae1edf68c
https://doi.org/10.1002/chin.199537139
https://doi.org/10.1002/chin.199537139
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e513634dfda80a5aba8af32aa898f91a
https://doi.org/10.1002/chin.199628171
https://doi.org/10.1002/chin.199628171
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:433-437
Stable nitrones are formed in the condensation of 5-hydroxylaminothiazolidine-2-thiones with 4-nitrobenzaldehyde. At the same time, nitrones obtained from the isomeric 4-hydroxylaminothiazolidine-2-thiones, as well as 4-hydroxylaminoimidazolidin-2-on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56a6ea57645fd855821b9ad1d0cbae18
https://doi.org/10.1007/bf00480846
https://doi.org/10.1007/bf00480846
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:823-827
Acylation with methyl chloroformate of N-monocarbamoyl derivatives of 4- and 5-hydroxylaminothiazolidin-2-thione and 4-hydroxylaminoimidazolidin-2-one, depending on their structure and the reaction conditions, leads either to N,O-bisacylhydroxylamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::237ab4a395923e5bee597697cbb6268b
https://doi.org/10.1007/bf00509717
https://doi.org/10.1007/bf00509717